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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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CoRoent® LI, 14x9x26mm 0°
Nuvasive, Inc.
6644926
In Commercial Distribution

  • 00887517334329 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LI, 12x9x26mm 0°
Nuvasive, Inc.
6642926
In Commercial Distribution

  • 00887517334312 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LI, 11x9x26mm 0°
Nuvasive, Inc.
6641926
In Commercial Distribution

  • 00887517334305 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LI, 10x9x26mm 0°
Nuvasive, Inc.
6640926
In Commercial Distribution

  • 00887517334091 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 9x14x40mm 0°
Nuvasive, Inc.
5494400
In Commercial Distribution

  • 00887517721181 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 9x14x35mm 0°
Nuvasive, Inc.
5494350
In Commercial Distribution

  • 00887517721136 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 8x14x35mm 0°
Nuvasive, Inc.
5484350
In Commercial Distribution

  • 00887517720733 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 8x14x30mm 0°
Nuvasive, Inc.
5484300
In Commercial Distribution

  • 00887517720689 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 8x14x25mm 0°
Nuvasive, Inc.
5484250
In Commercial Distribution

  • 00887517720634 ()


  • Polymeric spinal interbody fusion cage
Oblique TLIF Ti, 8x10x40mm 0°
Nuvasive, Inc.
5480400
In Commercial Distribution

  • 00887517720580 ()


  • Polymeric spinal interbody fusion cage
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